Division of Avian Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, the Chinese Academy of Agricultural Sciences, Harbin 150001, People's Republic of China.
Division of Avian Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, the Chinese Academy of Agricultural Sciences, Harbin 150001, People's Republic of China.
Vet Microbiol. 2013 Mar 23;162(2-4):429-436. doi: 10.1016/j.vetmic.2012.10.027. Epub 2012 Nov 1.
An infectious bronchitis virus (IBV), ck/CH/LZJ/111113, was isolated from a H120-vaccinated chicken which showed disease suspected of IBV infection. Neutralization testing showed that ck/CH/LZJ/111113 was distinct from either the Chinese predominant IBV LX4-type or Mass-type vaccine strains. Phylogenetic analysis confirmed that ck/CH/LZJ/111113 is of the 4/91 type; however, further extensive analyses of full-length genomes identified occurrence of recombination events. Therefore, ck/CH/LZJ/111113 originated from the recombination events between ck/CH/LDL/091022- and 4/91-like strains at three switch sites located upstream of the spike (S) glycoprotein gene, and the 3' ends of S1 and nuceocapsid (N) genes, respectively. The difference of serotypes and tissue tropisms in kidneys between ck/CH/LZJ/111113 and ck/CH/LDL/091022 may have been contributed by the uptake of the S1 gene by a ck/CH/LDL/091022-like virus from a 4/91-like strain. This recombination event took place at the 3' end of the N gene and the 3' untranslated region may account for differences in replication efficiency in tissues of chickens inoculated by the two viruses.
一株传染性支气管炎病毒(IBV),ck/CH/LZJ/111113,从一只接种 H120 疫苗的鸡中分离得到,该鸡表现出疑似 IBV 感染的疾病。中和试验表明,ck/CH/LZJ/111113 与中国主要的 IBV LX4 型或 Mass 型疫苗株不同。系统进化分析证实 ck/CH/LZJ/111113 属于 4/91 型;然而,对全长基因组的进一步广泛分析发现了重组事件的发生。因此,ck/CH/LZJ/111113 是由 ck/CH/LDL/091022-和 4/91 样株在三个开关位点之间发生重组事件而产生的,这三个开关位点分别位于 S 糖蛋白基因、S1 和核衣壳(N)基因的上游,以及 S1 和 N 基因的 3'末端。ck/CH/LZJ/111113 和 ck/CH/LDL/091022 在血清型和肾脏组织嗜性方面的差异可能是由于 ck/CH/LDL/091022 样病毒从 4/91 样株中摄取了 S1 基因所致。这种重组事件发生在 N 基因的 3'末端和 3'非翻译区,可能导致这两种病毒在接种鸡组织中的复制效率不同。